List of variants in gene XIAP reported as likely benign for Lymphoproliferative disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001167.4(XIAP):c.*1175ATTA[1]	rs747235601
NM_001167.4(XIAP):c.5034_5035insAAA	rs770819952
NM_001167.4(XIAP):c.*6564CTGA[2]	rs28382756

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